U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C16H19N3S.2BrH
Molecular Weight 447.231
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HYDROMETHYLTHIONINE DIHYDROBROMIDE

SMILES

Br.Br.CN(C)C1=CC2=C(NC3=C(S2)C=C(C=C3)N(C)C)C=C1

InChI

InChIKey=JAUPSVVTGFBHTN-UHFFFAOYSA-N
InChI=1S/C16H19N3S.2BrH/c1-18(2)11-5-7-13-15(9-11)20-16-10-12(19(3)4)6-8-14(16)17-13;;/h5-10,17H,1-4H3;2*1H

HIDE SMILES / InChI
L-MTX is a second-generation tau protein aggregation inhibitor. It acts by reducing levels of aggregated or misfolded tau proteins, which are associated with the progressive neurodegeneration. It is currently under development for the treatment of Alzheimer’s disease.

Approval Year

Targets

Targets

PubMed

PubMed

TitleDatePubMed
Tau-aggregation inhibitor therapy for Alzheimer's disease.
2014 Apr 15
Cellular Models of Aggregation-dependent Template-directed Proteolysis to Characterize Tau Aggregation Inhibitors for Treatment of Alzheimer Disease.
2015 Apr 24
Efficacy and safety of tau-aggregation inhibitor therapy in patients with mild or moderate Alzheimer's disease: a randomised, controlled, double-blind, parallel-arm, phase 3 trial.
2016 Dec 10
Patents

Sample Use Guides

L-MTX is given as a monotherapy at doses of 8 mg/day (taken as 4 mg twice daily) and of 16 mg/day (taken as 8 mg twice daily).
Route of Administration: Oral
Name Type Language
HYDROMETHYLTHIONINE DIHYDROBROMIDE
Common Name English
N3,N3,N7,N7-TETRAMETHYL-10H-PHENOTHIAZINE-3,7-DIAMINE DIHYDROBROMIDE
Systematic Name English
REDUCED METHYLENE BLUE DIHYDROBROMIDE
Common Name English
LEUCOMETHYLENE BLUE DIHYDROBROMIDE
Common Name English
LEUKOMETHYLENE BLUE DIHYDROBROMIDE
Common Name English
Code System Code Type Description
FDA UNII
E79ZM68IOZ
Created by admin on Sat Dec 16 11:50:42 GMT 2023 , Edited by admin on Sat Dec 16 11:50:42 GMT 2023
PRIMARY
SMS_ID
100000178330
Created by admin on Sat Dec 16 11:50:42 GMT 2023 , Edited by admin on Sat Dec 16 11:50:42 GMT 2023
PRIMARY
CAS
951131-15-0
Created by admin on Sat Dec 16 11:50:42 GMT 2023 , Edited by admin on Sat Dec 16 11:50:42 GMT 2023
PRIMARY
EVMPD
SUB194056
Created by admin on Sat Dec 16 11:50:42 GMT 2023 , Edited by admin on Sat Dec 16 11:50:42 GMT 2023
PRIMARY
PUBCHEM
23651551
Created by admin on Sat Dec 16 11:50:42 GMT 2023 , Edited by admin on Sat Dec 16 11:50:42 GMT 2023
PRIMARY